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Gpro

FDA UDI

Class I (US FDA UDI)

by Beyes Dental Canada Inc

Identity

Trade Name
GPRO FDA UDI
Generic Name
Endodontic obturation system handpiece, material extrusion FDA UDI
Device Name
GPRO F1,Gutta-percha Obturation Filling Machine Tips included: 1x 23G 24mm, 1x 23G 28mm, 2x 25G 24mm FDA UDI
Model / Reference
GP2002 FDA UDI
Description
GPRO F1,Gutta-percha Obturation Filling Machine Tips included: 1x 23G 24mm, 1x 23G 28mm, 2x 25G 24mm FDA UDI

Identifiers

Primary DI / UDI-DI
00837699001014 FDA UDI
FDA Product Code
EKR FDA UDI
GMDN Term
Endodontic obturation system handpiece, material extrusion FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Endodontic obturation system handpiece, material extrusion

Gpro by Beyes Dental Canada Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endodontic obturation system handpiece, material extrusion.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Beyes Dental Canada Inc

Sources (1)

  • FDA UDI fa65e43c-5e35-4bbe-93e6-b7388e134133 33 fields · synced May 29, 2026